Canonical Allele Identifier: CA385876059

Gene: PTPRQ

Linked Data

• ClinVar Variation Id: 3056886
• ClinVar RCV Id: RCV003973863
• MyVariant Identifiers: chr12:g.80460705G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460705G>A , CM000674.2:g.80460705G>A	GRCh38
NC_000012.11:g.80849472C>T , CM000674.1:g.80849472C>T	GRCh37
NC_000012.10:g.79373603C>T	NCBI36
NG_034052.1:g.21360G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.713G>A MANE Select	ENSP00000495607.1:p.Gly238Asp
ENST00000614701.4:c.713G>A	ENSP00000482885.1:p.Gly238Asp
ENST00000616559.4:c.839G>A	ENSP00000483259.1:p.Gly280Asp
NM_001145026.1:c.713G>A	NP_001138498.1:p.Gly238Asp
XM_011538290.1:c.713G>A	XP_011536592.1:p.Gly238Asp
XM_017019273.1:c.1379G>A	XP_016874762.1:p.Gly460Asp
XM_017019274.1:c.1379G>A	XP_016874763.1:p.Gly460Asp
XM_017019275.1:c.1379G>A	XP_016874764.1:p.Gly460Asp
XR_001748688.1:n.1516G>A
XR_001748689.1:n.1516G>A
NM_001145026.2:c.713G>A MANE Select	NP_001138498.1:p.Gly238Asp